Cornelia de Lange syndrome: A rare genetic disorder

Abstract

Cornelia de Lange Syndrome (CdLS) was first reported by Vrolik in 1849 and Brachmann in 1916, followed by Cornelia de Lange in 1933, after whom the syndrome is named. This disorder has a varied presentation but is mainly characterized by distinctive facial features, growth retardation, microcephaly, hirsutism, psychomotor delay, intellectual disability, and malformations of the upper limbs. Initial diagnosis is usually based on clinical features following specific diagnostic scoring systems. The precise prevalence of the disease is unknown but is estimated to be 1-10:100,000. Depending on the mutated gene, Cornelia de Lange syndrome (CdLS) can be inherited in an autosomal dominant manner, when it is caused by variations in the NIPBL, SMC2, or RAD21 genes, or it can have an X-linked inheritance when it is caused by variations in the SMC1A or HDAC8 genes.However, most cases (more than 99%) result from new (de novo) mutations, which means that are not inherited from the parents and occur in people with no family history of the conditionabout 30% of the people affected by the syndrome do not have any known cause. Many studies focused on the importance of neurologic findings and reported an incidence of epilepsy in CdLS ranging from 14% to 25%, especially in the classic and more severe form of the syndrome, but there is no data about its electroclinical features and long-term outcome. Life expectancy is relatively normal for people with CdLS and most affected children live well into adulthood. However, certain features of this condition, particularly severe malformations of the heart or throat, may decrease life expectancy in some affected people. The diagnosis is suspected clinically and later confirmed by clinical exome sequencing.

Scoping review of Physiotherapy intervention for a rare disease Cornelia de Lange Syndrome (CdLS)/ Brachman de Lange syndrome in children

“…The tests can help parents make decisions regarding additional testing, care, or treatment during pregnancy or after the baby is born. [6] The newest prenatal screening technique, non-invasive cell-free fetal DNA, can detect several genetic abnormalities in the growing baby in the mother's blood. This could be used to spot alterations in genes that could lead to CdLS.…”

“…Most children with CdLS caused by a shift in NIPBL can sit, walk independently, and begin to speak by the age of five. [6] When a family learns that their child has CdLS syndrome for the first time, whether during pregnancy or after birth, the truth may be more difficult and harsher, and the parents or one of them may have a negative attitude toward the child. A typical reaction to having everyone may expect all feelings, from wrath to anguish, remorse, shame, despair, and even refusal to accept the truth or kid.…”

“…The positive role of parents and their union, as well as the employment of psychologists and medical personnel, are all critical in reducing the severity of the trauma and making it acceptable to accept him as a family member. [6] Physiotherapy is an important component of a child's or adult's overall health and well-being. It has the potential to improve their movement and wellness.…”